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1
Q37132419-43764D9B-AD5B-46E5-AFA9-1E5DDB85E2E1
Q37132419-43764D9B-AD5B-46E5-AFA9-1E5DDB85E2E1
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http://www.wikidata.org/entity/statement/Q37132419-43764D9B-AD5B-46E5-AFA9-1E5DDB85E2E1
Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.
P2860
Q37132419-43764D9B-AD5B-46E5-AFA9-1E5DDB85E2E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37132419-43764D9B-AD5B-46E5-AFA9-1E5DDB85E2E1
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type
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Statement
wasDerivedFrom
c2785608bd2fc7b709b468f1506485d40cee722d
P2860
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.